Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: A4H605
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.420 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.405 |
DEG_MDM2_SWIB_1 | 302 | 310 | PF02201 | 0.474 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 383 | 393 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 414 | 422 | PF00069 | 0.469 |
DOC_MAPK_HePTP_8 | 341 | 353 | PF00069 | 0.218 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 344 | 353 | PF00069 | 0.218 |
DOC_PP1_RVXF_1 | 314 | 321 | PF00149 | 0.449 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.276 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.206 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.702 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.255 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.243 |
LIG_14-3-3_CanoR_1 | 169 | 176 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.595 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.755 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.280 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.352 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.251 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.282 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.575 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.555 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.267 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.338 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.638 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.757 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.730 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.222 |
LIG_GBD_Chelix_1 | 432 | 440 | PF00786 | 0.205 |
LIG_LIR_Gen_1 | 245 | 256 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 426 | 437 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 455 | 465 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 483 | 489 | PF02991 | 0.211 |
LIG_LIR_LC3C_4 | 252 | 257 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 252 | 256 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 345 | 349 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.298 |
LIG_PAM2_1 | 148 | 160 | PF00658 | 0.249 |
LIG_Pex14_1 | 342 | 346 | PF04695 | 0.289 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.282 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.282 |
LIG_Pex14_2 | 302 | 306 | PF04695 | 0.458 |
LIG_Rb_LxCxE_1 | 66 | 83 | PF01857 | 0.515 |
LIG_REV1ctd_RIR_1 | 300 | 308 | PF16727 | 0.329 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.338 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.255 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 322 | 325 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.205 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.205 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.227 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.613 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.697 |
LIG_SUMO_SIM_anti_2 | 293 | 299 | PF11976 | 0.243 |
LIG_SUMO_SIM_anti_2 | 496 | 501 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 434 | 439 | PF11976 | 0.295 |
LIG_TRAF2_1 | 15 | 18 | PF00917 | 0.639 |
LIG_TYR_ITIM | 145 | 150 | PF00017 | 0.338 |
LIG_TYR_ITSM | 380 | 387 | PF00017 | 0.198 |
LIG_UBA3_1 | 295 | 304 | PF00899 | 0.259 |
LIG_WRC_WIRS_1 | 213 | 218 | PF05994 | 0.321 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.338 |
LIG_WRC_WIRS_1 | 367 | 372 | PF05994 | 0.294 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.626 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.385 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.304 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.619 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.329 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.640 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.818 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.321 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.291 |
MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.486 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.466 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.344 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.406 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.460 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.568 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.373 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.276 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.333 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.479 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.285 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.264 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.337 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.275 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.460 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.319 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.241 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.378 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.373 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.464 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.394 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.544 |
MOD_NEK2_2 | 424 | 429 | PF00069 | 0.205 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.655 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.817 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.716 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.275 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.241 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.314 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.256 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.623 |
MOD_Plk_2-3 | 477 | 483 | PF00069 | 0.222 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.346 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.355 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.463 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.324 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.310 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.248 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.370 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.336 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.475 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.352 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.267 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.348 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.255 |
MOD_SUMO_rev_2 | 124 | 133 | PF00179 | 0.588 |
MOD_SUMO_rev_2 | 186 | 192 | PF00179 | 0.242 |
TRG_DiLeu_BaEn_1 | 483 | 488 | PF01217 | 0.338 |
TRG_DiLeu_BaEn_4 | 17 | 23 | PF01217 | 0.637 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6X2 | Leptomonas seymouri | 60% | 100% |
A0A0N1PC74 | Leptomonas seymouri | 26% | 100% |
A0A0N1PCA2 | Leptomonas seymouri | 28% | 100% |
A0A3Q8I8Q6 | Leishmania donovani | 71% | 100% |
A0A3S7WR28 | Leishmania donovani | 27% | 100% |
A0A3S7X1E1 | Leishmania donovani | 29% | 98% |
A4H606 | Leishmania braziliensis | 24% | 100% |
A4HGF8 | Leishmania braziliensis | 27% | 97% |
A4HUD2 | Leishmania infantum | 71% | 100% |
A4HUD3 | Leishmania infantum | 27% | 100% |
A4I3I9 | Leishmania infantum | 29% | 98% |
E9AN32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9AN33 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AZT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 97% |
Q4Q8F3 | Leishmania major | 28% | 100% |
Q4QHJ3 | Leishmania major | 27% | 100% |
Q4QHJ4 | Leishmania major | 70% | 96% |